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Articles

‘Finding the needle in the haystack’- will natural products fit for purpose in the treatment of cryptosporidiosis? – A theoretical perspective

ORCID Icon, , & ORCID Icon
Pages 636-649 | Received 07 Dec 2020, Accepted 16 Feb 2021, Published online: 03 Mar 2021
 

ABSTRACT

The limitations that have inundated mainstream anticryptosporidials have necessitated the exploration of alternative approaches towards the design of novel anticryptosporidials with improved therapeutic activity. We virtually screened a dedicated library of 107,000 natural compounds available in the ZINC database against Cryptosporidium parvum inosine monophosphate dehydrogenase-NAD+ binding site. The top three compounds identified with the best complementarity to the CpIMPDH-NAD+ binding site included ZINC5225833, ZINC4258873, and ZINC3841381. Estimation of the total binding free energy using Molecular Mechanics Generalized Poisson Boltzmann Surface Area (MM/PBSA) method had the three compounds eliciting favourable binding free energies. ZINC3841381 had the best binding free energy of −58.43 kcal/mol followed by ZINC4258873 with −51.1 kcal/mol and ZINC5225833, −38.04 kcal/mol. The binding of the natural compounds to CpIMPDH induced structural perturbations in the protein compared to the apo. We evaluated the compliance of the natural compounds to Lipinski's rule of 5 and other pharmacokinetic parameters. From this evaluation, the natural compounds are drug-likely but can still make do with some modifications to improve their therapeutic potentials. The results obtained from this study can serve as a preliminary background in the further experimental exploration of ZINC5225833, ZINC4258873, and ZINC3841381 as potential anticryptosporidials.

Acknowledgement

We acknowledge the Centre for High Performance Computing, Cape Town for computational resources.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Data availability statement

All data generated in this study are included in this manuscript and its supplementary file.

Additional information

Funding

The authors received no financial support for the study.

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